Coulombe P, Schwartz H L, Oppenheimer J H
J Clin Invest. 1978 Nov;62(5):1020-8. doi: 10.1172/JCI109206.
Studies were undertaken in hypothyroid rats in an effort to define the kinetics of growth hormone (GH) accumulation in response to i.v. pulse injections of triiodothyronine (T(3)) and to calculate the relationship between nuclear occupancy by T(3) and the instantaneous rate of accumulation of pituitary GH. Results were contrasted to the findings in previous studies of the induction of hepatic mitochondrial alpha-glycerophosphate dehydrogenase (alpha-GPD) and malic enzyme (ME) by T(3). The dose of T(3) required to achieve half-maximal accumulation of GH in 24 h was 0.6 mug/100 g body wt, a value 15-fold less than the half-maximal dose for alpha-GPD and ME induction at a comparable time after injection. Although significant increase in pituitary GH were evident as early as 3 h after injection of maximally effective doses of T(3), the rate of increase became linear only 12 h after injection. After achievement of peak values, the pituitary content of GH decayed with a similar terminal t((1/2)) of 3.9 days and 4.1 days in two groups of animals injected with a single dose of 1.0 and 50 mug T(3)/100 g body wt, respectively. In vivo isotopic displacement studies carried out at the equilibrium time point indicated that the pituitary nuclear binding capacity was 5.5 ng T(3)/g tissue and that the plasma concentration at which one-half of the nuclear sites are occupied is 1.0 ng/ml. Nuclear occupancy as a function of time was calculated from the estimated plasma T(3) concentration after injection of the dose and the half-occupancy plasma concentration. These data were then analyzed by application of the mathematical model previously developed to ascertain the relationship between nuclear occupancy and the rate of hepatic enzyme induction. Results indicated that the pituitary nuclear occupancy-response relationship was generally linear, in marked contrast to the highly amplified relationship between nuclear occupancy and the response of ME and alpha-GPD to T(3) in the liver. In supplementary experiments, euthyroid rats received daily injections of 200 mug of T(3) for 7 days to keep nuclear sites nearly saturated for the duration of the experiment. No significant increase in the pituitary GH content above euthyroid base-line levels was noted. This also contrasts with the marked increase above euthyroid levels in alpha-GPD and ME observed in previous studies. Our findings suggest the existence of major differences between the specific mechanisms which lead to the induction of pituitary GH and the hepatic enzymes by T(3).
在甲状腺功能减退的大鼠身上进行了研究,旨在确定静脉脉冲注射三碘甲状腺原氨酸(T3)后生长激素(GH)积累的动力学,并计算T3在细胞核中的占有率与垂体GH瞬时积累速率之间的关系。将结果与先前关于T3诱导肝线粒体α-甘油磷酸脱氢酶(α-GPD)和苹果酸酶(ME)的研究结果进行对比。在24小时内使GH积累达到最大值一半所需的T3剂量为0.6微克/100克体重,该值比注射后相当时间诱导α-GPD和ME达到最大值一半的剂量低15倍。尽管在注射最大有效剂量的T3后3小时,垂体GH就明显显著增加,但增加速率仅在注射后12小时才变为线性。达到峰值后,在分别注射1.0微克和50微克T3/100克体重单剂量的两组动物中,垂体GH含量以相似的终末半衰期3.9天和4.1天下降。在平衡时间点进行的体内同位素置换研究表明,垂体细胞核结合能力为5.5纳克T3/克组织,占据一半细胞核位点的血浆浓度为1.0纳克/毫升。根据注射剂量后估计的血浆T3浓度和占据一半位点的血浆浓度计算出细胞核占有率随时间的变化。然后应用先前开发的数学模型对这些数据进行分析,以确定细胞核占有率与肝酶诱导速率之间的关系。结果表明,垂体细胞核占有率-反应关系通常是线性的,这与肝脏中细胞核占有率与ME和α-GPD对T3反应之间的高度放大关系形成显著对比。在补充实验中,甲状腺功能正常的大鼠每天注射200微克T3,持续7天,以使细胞核位点在实验期间几乎饱和。未观察到垂体GH含量比甲状腺功能正常的基线水平有显著增加。这也与先前研究中观察到的α-GPD和ME比甲状腺功能正常水平显著增加形成对比。我们的研究结果表明,T3诱导垂体GH和肝酶的具体机制之间存在重大差异。